RWE and HEOR Statistician/Programmer

Apr; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

A leading company is seeking a highly skilled Consultant Statistician/Programmer for a remote, 12-month renewable contract. The role involves supporting Real-World Evidence and Health Economics initiatives by developing statistical programs using SAS and R, collaborating with biostatisticians, and ensuring compliance with industry standards. Ideal candidates will have a Master's degree in a relevant field and significant experience in clinical research.

Qualifications

• Minimum of 4 years of experience in clinical research.
• Hands-on experience with CDISC SDTM and ADaM datasets.
• Proficiency in SAS and R programming required.

Responsibilities

• Develop, validate, and maintain SAS and/or R programs for statistical analyses.
• Collaborate with biostatisticians on various projects.
• Perform quality control on statistical programs and outputs.

Skills

Analytical skills

Problem-solving skills

Statistical techniques

Data quality checks

Education

Master’s degree in Statistics, Biostatistics, Mathematics, Computer Science

Tools

SAS

R

Job description

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Remote, 12-month renewable contract

Position Summary:

We are seeking a highly skilled and detail-oriented Consultant Statistician/Programmer to support Real-World Evidence (RWE) and Health Economics and Outcomes Research (HEOR) initiatives. The successful candidate will work closely with the RWE/HEOR biostatistician and will be responsible for developing, executing, and validating statistical programs using SAS and/or R to support analyses and deliverables for RWE, HEOR, and Market Access activities.

Responsibilities:

• Collaborate with HEOR and RWE biostatisticians to provide statistical programming support across various projects.
• Develop, validate, and maintain SAS and/or R programs to support statistical analyses and reporting activities for HEOR, RWE, and Market Access studies.
• Generate high-quality tables, listings, and figures based on clinical trial data and other relevant data sources.
• Perform statistical modeling and analyses as required.
• Utilize SDTM and ADaM datasets to derive analysis datasets.
• Serve as the primary programmer on assigned projects, ensuring that programming deliverables are accurate and consistent.
• Perform quality control (QC) on statistical programs and outputs as needed.
• Ensure all programming activities comply with industry standards, study protocols, and statistical analysis plans (SAPs).
• Provide input on statistical methodologies and contribute to project deliverables.
• Maintain comprehensive documentation and audit trails for all programming activities.
• Perform rigorous data quality checks to ensure accuracy, completeness, and consistency.

Education & Experience Requirements:

• Master’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related technical discipline.
• Minimum of 4 years of experience in clinical research, preferably within the pharmaceutical or CRO industry, with exposure to Phase I–IV trials.
• Hands-on experience with CDISC SDTM and ADaM datasets.
• Proficiency in SAS and R programming is required

Additional Skills & Experience:

• Strong analytical and problem-solving skills, with the ability to manage complex studies and meet deadlines.
• Experience with statistical techniques, including longitudinal data analysis, survival analysis, and statistical modeling/simulation.
• Familiarity with observational studies, causal inference, patient-reported outcomes (PROs), and health technology assessment (HTA)
• Experience with indirect treatment comparisons (ITCs), such as matching-adjusted indirect comparison (MAIC), is a plus.
• Prior experience in a similar role within the pharmaceutical industry, preferably with a focus on small molecule pharmaceuticals.

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